US7462574B2 - Silica glass containing TiO2 and optical material for EUV lithography - Google Patents

Silica glass containing TiO2 and optical material for EUV lithography Download PDF

Info

Publication number
US7462574B2
US7462574B2 US11/174,533 US17453305A US7462574B2 US 7462574 B2 US7462574 B2 US 7462574B2 US 17453305 A US17453305 A US 17453305A US 7462574 B2 US7462574 B2 US 7462574B2
Authority
US
United States
Prior art keywords
tio
glass
sio
fluctuation
refractive index
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US11/174,533
Other languages
English (en)
Other versions
US20050245383A1 (en
Inventor
Yasutomi Iwahashi
Akio Koike
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
AGC Inc
Original Assignee
Asahi Glass Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=33162776&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=US7462574(B2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Asahi Glass Co Ltd filed Critical Asahi Glass Co Ltd
Assigned to ASAHI GLASS COMPANY, LIMITED reassignment ASAHI GLASS COMPANY, LIMITED ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: IWAHASHI, YASUTOMI, KOIKE, AKIO
Publication of US20050245383A1 publication Critical patent/US20050245383A1/en
Application granted granted Critical
Publication of US7462574B2 publication Critical patent/US7462574B2/en
Assigned to AGC Inc. reassignment AGC Inc. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: ASAHI GLASS COMPANY, LIMITED
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C3/00Glass compositions
    • C03C3/04Glass compositions containing silica
    • C03C3/06Glass compositions containing silica with more than 90% silica by weight, e.g. quartz
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B19/00Other methods of shaping glass
    • C03B19/14Other methods of shaping glass by gas- or vapour- phase reaction processes
    • C03B19/1484Means for supporting, rotating or translating the article being formed
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C4/00Compositions for glass with special properties
    • C03C4/0085Compositions for glass with special properties for UV-transmitting glass
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03BMANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
    • C03B2201/00Type of glass produced
    • C03B2201/06Doped silica-based glasses
    • C03B2201/30Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi
    • C03B2201/40Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi doped with transition metals other than rare earth metals, e.g. Zr, Nb, Ta or Zn
    • C03B2201/42Doped silica-based glasses doped with metals, e.g. Ga, Sn, Sb, Pb or Bi doped with transition metals other than rare earth metals, e.g. Zr, Nb, Ta or Zn doped with titanium
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2201/00Glass compositions
    • C03C2201/06Doped silica-based glasses
    • C03C2201/30Doped silica-based glasses containing metals
    • C03C2201/40Doped silica-based glasses containing metals containing transition metals other than rare earth metals, e.g. Zr, Nb, Ta or Zn
    • C03C2201/42Doped silica-based glasses containing metals containing transition metals other than rare earth metals, e.g. Zr, Nb, Ta or Zn containing titanium

Definitions

  • the present invention relates to a silica glass containing TiO 2 (hereinafter referred to as TiO 2 —SiO 2 glass) and a process for its production. Particularly, it relates to TiO 2 —SiO 2 glass to be used for an optical material for an exposure device to be used for EUV lithography and a process for its production.
  • EUV (Extreme Ultra Violet) light means light having a waveband in a soft X-ray region or in a vacuum ultraviolet region and specifically means light having a wavelength of from 0.2 to 100 nm.
  • an exposure device to transfer a fine circuit pattern onto a wafer to produce an integrated circuit.
  • microsizing of integrated circuit has been progressing, and an exposure device is required to form an image of a circuit pattern on a wafer with a high resolution in a deep focal depth, whereby blue shift of the exposure light source is in progress.
  • the exposure light source has been advanced from the conventional g-line (wavelength: 436 nm), i-line (wavelength: 365 nm) or KrF excimer laser (wavelength: 248 nm), and now an ArF excimer laser (wavelength: 193 nm) is being used.
  • EUVL extreme ultraviolet light
  • the optical material for the exposure device to be used for EUVL will be a photomask, a mirror or the like, and it is basically constituted of (1) a base material, (2) a reflective multilayer formed on the base material and (3) an absorber layer formed on the reflective multilayer.
  • a base material For the multilayer, it is studied to form layers of Mo/Si alternately, and for the absorber layer, it is studied to use Ta or Cr as the layer-forming material.
  • the base material a material having a low thermal expansion coefficient is required so that no strain will be formed even under irradiation with EUV light, and a glass having a low thermal expansion coefficient is being studied.
  • TiO 2 —SiO 2 glass is known to be a very low thermal expansion material having a coefficient of thermal expansion (CTE) smaller than quartz glass, and the coefficient of thermal expansion can be controlled by the TiO 2 content in the glass, whereby it is possible to obtain a zero expansion glass having a coefficient of thermal expansion being close to zero. Accordingly, TiO 2 —SiO 2 glass is prospective as a material to be used for an optical material for the exposure device for EUVL.
  • CTE coefficient of thermal expansion
  • TiO 2 —SiO 2 glass In a conventional method for preparing TiO 2 —SiO 2 glass, firstly, a silica precursor and a titania precursor are, respectively, converted into a vapor form, and then mixed. Such a vapor form mixture is feeded into a burner and thermally decomposed to form TiO 2 —SiO 2 glass particles. Such TiO 2 —SiO 2 glass particles will be deposited in a refractory container and at the same time will be melted to form TiO 2 —SiO 2 glass.
  • TiO 2 —SiO 2 glass prepared by this method has had a periodical fluctuation of the TiO 2 /SiO 2 ratio, which appears as striped striae with a 100 to 200 ⁇ m pitch.
  • U.S. patent application publication No. 2002/157421 discloses a method which comprises forming a TiO 2 —SiO 2 porous glass body, converting it to a glass body, and then obtaining a mask substrate therefrom.
  • the striped striae of the TiO 2 —SiO 2 glass are considered to form as the difference in the refractive index increases due to the periodical fluctuation of the TiO 2 /SiO 2 ratio in the glass material.
  • the TiO 2 —SiO 2 glass is required to be polished so that the glass will have an ultra smooth surface.
  • the mechanical and chemical properties of the glass vary depending upon the composition, whereby the polishing rate tends to be non-uniform, and it is difficult to finish so that the glass surface after polishing will be ultra smooth.
  • MSFR Mobile-Spatial Frequency Roughness
  • the TiO 2 /SiO 2 ratio it is important to make the TiO 2 /SiO 2 ratio uniform in the TiO 2 —SiO 2 glass, with a view to minimizing the fluctuation of the coefficient of thermal expansion within the glass. Accordingly, in addition to minimizing the fluctuation of the TiO 2 /SiO 2 ratio in the small areas so-called striae, it is preferred to minimize the fluctuation of the TiO 2 /SiO 2 ratio in the entire region of the material.
  • Embodiment 1 of the present invention provides a silica glass containing TiO 2 , characterized in that the fluctuation of the refractive index ( ⁇ n) is at most 2 ⁇ 10 ⁇ 4 within an area of 30 mm ⁇ 30 mm in at least one plane.
  • Embodiment 2 provides the silica glass containing TiO 2 according to Embodiment 1, wherein the fluctuation of the refractive index ( ⁇ n) is at most 2 ⁇ 10 ⁇ 4 within an area of 30 mm ⁇ 30 mm in each of two orthogonal planes.
  • Embodiment 3 provides a silica glass containing TiO 2 , characterized in that the TiO 2 concentration is at least 1 mass %, and the difference between the maximum value and the minimum value of the TiO 2 concentration is at most 0.06 mass % within an area of 30 mm ⁇ 30 mm in at least one plane.
  • Embodiment 4 provides the silica glass containing TiO 2 according to Embodiment 3, wherein the difference between the maximum value and the minimum value of the TiO 2 concentration is at most 0.06 mass % within an area of 30 mm ⁇ 30 mm in each of two orthogonal planes.
  • Embodiment 5 provides a silica glass containing TiO 2 , characterized in that the TiO 2 concentration is at least 1 mass %, and the striae pitch is at most 10 ⁇ m.
  • Embodiment 6 provides the silica glass containing TiO 2 according to Embodiment 1, 2, 3 or 4, wherein the striae pitch is at most 10 ⁇ m.
  • Embodiment 7 provides an optical material for EUV lithography, characterized in that it is made of a silica glass containing TiO 2 , and the fluctuation of the refractive index ( ⁇ n) is at most 2 ⁇ 10 ⁇ 4 in a plane perpendicular to the incident light direction.
  • Embodiment 8 provides the optical material for EUV lithography according to Embodiment 7, wherein there is no striae which cause a fluctuation of the refractive index ( ⁇ n) exceeding 2 ⁇ 10 ⁇ 4 in a plane perpendicular to the incident light direction.
  • Embodiment 9 provides an optical material for EUV lithography, characterized in that it is made of a silica glass containing TiO 2 , wherein the TiO 2 concentration is at least 1 mass %, and the difference between the maximum value and the minimum value of the TiO 2 concentration is at most 0.06 mass % in a plane perpendicular to the incident light direction.
  • Embodiment 10 provides the optical material for EUV lithography according to Embodiment 9, wherein there is no striae which cause a difference between the maximum value and the minimum value of the TiO 2 concentration, exceeding 0.06 mass % in a plane perpendicular to the incident light direction.
  • Embodiment 11 provides the optical material for EUV lithography according to any one of Embodiments 6 to 10, wherein the striae pitch is at most 10 ⁇ m.
  • Embodiment 12 provides an optical material for EUV lithography employing the silica glass containing TiO 2 , as defined in any one of Embodiments 1 to 6.
  • TiO 2 —SiO 2 glass having a small surface roughness. Accordingly, it is very useful as a material for a component constituting an optical system to be used for EUVL.
  • TiO 2 —SiO 2 glass is known to have a coefficient of thermal expansion which changes depending upon the concentration of TiO 2 contained, and the coefficient of thermal expansion of TiO 2 —SiO 2 glass containing about 7 mass % of TiO 2 becomes substantially zero at near room temperature.
  • the TiO 2 —SiO 2 glass of the present invention is preferably a silica glass containing from 1 to 12 mass % of TiO 2 . If the content of TiO 2 is less than 1%, zero expansion may not be accomplished, and if it exceeds 12 mass %, the coefficient of thermal expansion is likely to be negative. The content of TiO 2 is more preferably from 5 to 9 mass %.
  • the striae pitch is preferably at most 10 ⁇ m, more preferably at most 7 ⁇ m. If the striae pitch exceeds 10 ⁇ m, it tends to be difficult to reduce MSFR of the polished surface.
  • the fluctuation of the TiO 2 concentration is defined to be the difference between the maximum value and the minimum value of the TiO 2 concentration in one plane.
  • the fluctuation of the TiO 2 concentration in each area of 30 mm ⁇ 30 mm, that is small area, is preferably at most 0.06 mass %, more preferably at most 0.04 mass %. If the fluctuation of the TiO 2 concentration exceeds 0.06 mass %, it tends to be difficult to obtain an adequate smoothness by polishing.
  • a process for producing a TiO 2 —SiO 2 glass having the fluctuation of the TiO 2 concentration controlled to be within 0.06 mass % is as follows.
  • TiO 2 —SiO 2 glass particles (soot) obtained by flame hydrolysis or thermal decomposition of a Si precursor and a Ti precursor as glass-forming materials, by a soot process, are deposited and grown on a target to obtain a porous TiO 2 —SiO 2 glass body, and the obtained porous TiO 2 —SiO 2 glass body is heated to a vitrification temperature to obtain a verified TiO 2 —SiO 2 glass body.
  • the target made of quartz glass may, for example, be used for this process.
  • the present inventors have investigated the relationship between the rotational speed of the target in the step of obtaining the porous TiO 2 —SiO 2 glass body and the striae pitch of the obtained TiO 2 —SiO 2 glass body in detail. As a result, they have found that as the rotational speed of the target becomes high, the fluctuation of the TiO 2 concentration in the TiO 2 —SiO 2 glass body becomes small, and the striae pitch is reduced.
  • a rotational speed of the target at the step of obtaining the porous TiO 2 —SiO 2 glass body is preferably adjusted to be at least 25 rpm, more preferably at least 50 rpm, particularly preferably at least 100 rpm.
  • the fluctuation of the TiO 2 concentration in the TiO 2 —SiO 2 glass body will be at most 0.06 mass %, and the striae pitch will be at most 10 ⁇ m by this method.
  • the striae observed in a TiO 2 —SiO 2 glass are attributable to the fluctuation of the TiO 2 /SiO 2 ratio. Further, if the TiO 2 /SiO 2 ratio fluctuates, the absolute refractive index of glass will fluctuate. For example, at a portion where the TiO 2 concentration is high, the refractive index tends to be high as compared with a portion where the TiO 2 concentration is low.
  • the present inventors have measured the absolute refractive indices of several TiO 2 —SiO 2 glasses having different TiO 2 concentrations and have found that the following relation is satisfied between the TiO 2 concentration and the refractive index within a range where the TiO 2 concentration is at most 12 mass %.
  • Absolute refractive index 3.27 ⁇ 10 ⁇ 3 ⁇ TiO 2 concentration(mass %)+1.459 (1)
  • the formula (1) it will be possible to calculate the fluctuation of the TiO 2 concentration ( ⁇ TiO 2 ) from the fluctuation of the refractive index ( ⁇ n) of the TiO 2 —SiO 2 glass. Specifically, when the fluctuation of the refractive index ( ⁇ n) is 200 ppm, the fluctuation of the TiO 2 concentration ( ⁇ TiO 2 ) is 0.06 mass %.
  • the method of obtaining the striae pitch is as follows.
  • the fluctuation of the refractive index ( ⁇ n) in the plane is measured, and the distance from the portion where the refractive index is high to the portion where the refractive index is low, is measured by means of a microscope.
  • the method for measuring the fluctuation of the refractive index ( ⁇ n) is different as between the case of the fluctuation of the refractive index in small areas ( ⁇ n 1 ), and the case of the fluctuation of the refractive index in a broad area ( ⁇ n 2 ), as shown hereinafter.
  • the fluctuation of the refractive index in small areas ( ⁇ n 1 ) so-called striae is measured as follows. From the TiO 2 —SiO 2 glass body, a cube of about 40 mm ⁇ 40 mm ⁇ 40 mm is, for example, cut out, and each side of the cube is sliced in a thickness of 1 mm to obtain a plate-shaped TiO 2 —SiO 2 glass block of 30 mm ⁇ 30 mm ⁇ 1 mm.
  • a helium neon laser beam is vertically irradiated to an area of 30 mm ⁇ 30 mm of this glass block, and the refractive index distribution within the area is examined by magnifying to 2 mm ⁇ 2 mm, for example, where the striae can be sufficiently observed, and the fluctuation of the refractive index ( ⁇ n) is measured.
  • the entire area of 30 mm ⁇ 30 mm is divided into a lot of small areas at a level of, for example, 2 mm ⁇ 2 mm, and the fluctuation of the refractive index ( ⁇ n 1 ) in each small area, is measured, and the maximum value is taken as the fluctuation of the refractive index ( ⁇ n) in an area of 30 mm ⁇ 30 mm.
  • one pixel corresponds to about 4 square ⁇ m in a visual field of 2 mm ⁇ 2 mm. Accordingly, striae with a pitch of at least 10 ⁇ m can be sufficiently detected, but striae smaller than this may not be detected sometime. Therefore, in a case where striae of at most 10 ⁇ m are to be measured, it is advisable to set at least that one pixel corresponds to at most 1 to 2 square ⁇ m. In Examples in this specification, the fluctuation of the refractive index ( ⁇ n 1 ) was measured so that one pixel corresponds to about 2 square ⁇ m by measuring an area of 2 mm ⁇ 2 mm by means of CCD having 900 ⁇ 900 valid pixels.
  • the fluctuation of the refractive index in a broad area such as an area irradiated with EUV light to be used for exposure is measured as follows.
  • a formed TiO 2 —SiO 2 glass body of 160 mm ⁇ 160 mm ⁇ 150 mm is sliced into a block of 7 mm in thickness to obtain a TiO 2 —SiO 2 glass block of 160 mm ⁇ 160 mm ⁇ 7 mm.
  • a helium neon laser beam is vertically irradiated to the face of 160 mm ⁇ 160 mm of this glass block, and the refractive index distribution within an area of 100 mm ⁇ 100 mm is examined, and the fluctuation of the refractive index ( ⁇ n 2 ) is measured.
  • the fluctuation of the refractive index ( ⁇ n 2 ) was measured so that one pixel corresponds to about 300 to 400 square ⁇ m by measuring an area of 100 mm ⁇ 100 mm by means of CCD having 320 ⁇ 240 valid pixels.
  • the refractive index difference in an area of about 1 mm can be measured.
  • the absolute value of the refractive index can not be measured, and only the refractive index difference can be obtained. Accordingly, if the divided small areas are measured without directly measuring the entire area irradiated with EUV light to be used for exposure, the refractive indices at both ends of the material can not be compared, and it is possible that the fluctuation of the refractive index is estimated to be small. Therefore, the fluctuation of the refractive index is measured over the entire area irradiated with EUV light to be used for exposure, and the measured value is taken as the fluctuation of the refractive index in a plane perpendicular to the incident direction ( ⁇ n).
  • the fluctuation of the refractive index in small areas is measured by the above-mentioned method on the same face, if the fluctuation of the refractive index in the small areas ( ⁇ n 1 ) is larger than the fluctuation of the refractive index in the entire area ( ⁇ n 2 ), the fluctuation of the refractive index in the small areas ( ⁇ n 1 ) is taken as the fluctuation of the refractive index in the plane perpendicular to the incident direction ( ⁇ n).
  • the TiO 2 /SiO 2 ratio it is very important to make the TiO 2 /SiO 2 ratio uniform in a broad area such as an area irradiated with EUV light to be used for exposure when the TiO 2 —SiO 2 glass is used as a material for the exposure device for EUVL, with a view to minimizing the fluctuation of the coefficient of the thermal expansion within the material.
  • This fluctuation of the TiO 2 /SiO 2 ratio causes the refractive index of glass. Accordingly, the fluctuation of the refractive index may be used as an index for the uniformity of the TiO 2 —SiO 2 composition.
  • ⁇ n in the plane perpendicular to the incident light direction is preferably within a range of 2 ⁇ 10 ⁇ 4 , more preferably within 1.5 ⁇ 10 ⁇ 4 , particularly preferably within 1.0 ⁇ 10 ⁇ 4 .
  • ⁇ n in an area of 30 mm ⁇ 30 mm is preferably within 2 ⁇ 10 ⁇ 4 , more preferably within 1.5 ⁇ 10 ⁇ 4 , particularly preferably within 1.0 ⁇ 10 ⁇ 4 , most preferably within 0.5 ⁇ 10 ⁇ 4 . If ⁇ n exceeds the above range, the polishing rate will not be constant depending upon the position, and it tends to be difficult to finish so that the glass surface after polishing will be ultra smooth surface.
  • the TiO 2 —SiO 2 glass having a striae pitch of at most 10 ⁇ m or the TiO 2 —SiO 2 glass of which a fluctuation of the TiO 2 concentration is at most 0.06 mass %, obtained by the present invention is cut into a size of 160 mm ⁇ 160 mm ⁇ 7 mm, and then, an area of 160 mm ⁇ 160 mm is polished, the value of MSFR (Mid-Spatial Frequency Roughness) which has a waving pitch within a range of from 10 ⁇ m to 1 mm and is an index showing smoothness of a polished surface, will be a roughness (rms) of at most 1.5 nm, which is suitable for an optical material for the exposure device for EUVL.
  • MSFR Mod-Spatial Frequency Roughness
  • the TiO 2 —SiO 2 glass having a striae pitch of at least 10 ⁇ m or the TiO 2 —SiO 2 glass having a fluctuation of the TiO 2 concentration being at least 0.06 mass % it is difficult to bring MSFR of the polished surface to be at most 1.5 nm, whereby such a glass tends to be inadequate for an optical material for the exposure device for EUVL.
  • the fluctuation of the TiO 2 /SiO 2 ratio or An usually becomes largest at the portion having the striae. Accordingly, in such a case, if the fluctuation of the refractive index or the fluctuation of the TiO 2 /SiO 2 ratio is reduced in an area of 30 mm ⁇ 30 mm in at least one plane, by reducing the degree of the striae, it is possible to reduce the fluctuation of the TiO 2 /SiO 2 ratio or the fluctuation of the refractive index in each of two orthogonal planes simultaneously.
  • the TiO 2 —SiO 2 glass of the present invention By using the TiO 2 —SiO 2 glass of the present invention, it becomes easy to obtain an optical material for EUV lithography, which is made of the TiO 2 —SiO 2 glass and wherein the fluctuation of the refractive index ( ⁇ n) is at most 2 ⁇ 10 ⁇ 4 in a plane perpendicular to the incident light direction.
  • the degree of the striae itself is reduced, whereby it is possible to easily obtain an optical material for EUV lithography which is made of the TiO 2 —SiO 2 glass and wherein the striae are not present which cause the fluctuation of the refractive index ( ⁇ n) to exceed 2 ⁇ 10 ⁇ 4 in a plane perpendicular to the incident light direction.
  • the TiO 2 —SiO 2 glass of the present invention it is possible to easily obtain an optical material for EUV lithography which is made of the TiO 2 —SiO 2 glass having a TiO 2 concentration of at least 1 mass % and wherein the difference between the maximum value and the minimum value of the TiO 2 concentration is at most 0.06 mass %, in a plane perpendicular to the incident light direction.
  • an optical material for EUV lithography which is made of the TiO 2 —SiO 2 glass having a TiO 2 concentration of at least 1 mass % and wherein the striae are not present which cause the difference between the maximum value and the minimum value of the TiO 2 concentration to exceed 0.06 mass % in a plane perpendicular to the incident light direction.
  • the TiO 2 —SiO 2 glass can be made to be a zero expansion glass, of which the coefficient of thermal expansion is within a range of 0 ⁇ 200 ppb/° C.
  • the temperature range wherein the coefficient of the thermal expansion shows substantially zero can be made wider.
  • the coefficient of the thermal expansion can be made to be within a range of 0 ⁇ 200 ppb/° C.
  • the optical material for EUVL when the optical material for EUVL is prepared, by adjusting so that striae will be parallel to patterning surface, it is also possible to reduce the fluctuation of the TiO 2 /SiO 2 ratio or the fluctuation of the refractive index in a plane perpendicular to the incident light direction and to reduce MSFR.
  • the coefficient of thermal expansion is measured within a range of from ⁇ 150 to +200° C. by means of a laser interferometer type expansion meter (LIX-1, by manufactured by ULVAC-RIKO, Inc.).
  • LIX-1 laser interferometer type expansion meter
  • the fluctuation of the coefficient of thermal expansion is measured as follows.
  • a TiO 2 —SiO 2 glass block of 160 mm ⁇ 160 mm ⁇ 150 mm is cut and divided into small pieces of TiO 2 —SiO 2 glass of 20 mm ⁇ 20 mm ⁇ 10 mm.
  • the coefficient of thermal expansion of each small piece is measured in accordance with the above-mentioned method, to obtain the fluctuation of the coefficient of thermal expansion of the TiO 2 —SiO 2 glass block of 160 mm ⁇ 160 mm ⁇ 30 mm.
  • the optical material for EUV lithography is required to have a small fluctuation of the coefficient of thermal expansion.
  • the difference between the maximum value and the minimum value of the TiO 2 concentration is at most 0.06 mass %, so the fluctuation of the coefficient of thermal expansion of the TiO 2 —SiO 2 glass of the present invention obtained by a calibration curve will be at most about ⁇ 5 ppb/° C. at room temperature.
  • the TiO 2 —SiO 2 glass of the present invention can be made to have a fluctuation of the coefficient of thermal expansion being, for example, at most ⁇ 5 ppb/° C. at room temperature, and as such, is suitable for an optical material for EUV lithography.
  • the following process can be employed for producing the TiO 2 —SiO 2 glass of the present invention.
  • TiO 2 —SiO 2 glass particles obtained by flame hydrolysis of a Si precursor and a Ti precursor as glass-forming materials, are deposited and grown on a rotating target to obtain a porous TiO 2 —SiO 2 glass body (the target as disclosed, for example, in JP-B-63-24973).
  • the glass-forming materials are not particularly limited so long as they are materials capable of being gasified.
  • the Si precursor may, for example, be a silicon halide compound, such as a chloride such as SiCl 4 , SiHCl 3 , SiH 2 Cl 2 or SiH 3 Cl, a fluoride such as SiF 4 , SiHF 3 or SiH 2 F 2 , a bromide such as SiBr 4 or SiHBr 3 or an iodide such as SiI 4 , or an alkoxy silane represented by R n Si(OR) 4 ⁇ n (wherein R is a C 1-4 alkyl group, and n is an integer of from 0 to 3), and the Ti precursor may, for example, be a titanium halide compound such as TiCl 4 or TiBr 4 , or a titanium alkoxide represented by R n Si(OR) 4 ⁇ n (wherein R is a C 1-4 alkyl group, and n is an integer of from 0 to 3).
  • a silicon halide compound such as a chloride such as SiCl 4 , SiHCl 3
  • the Si precursor and the Ti precursor a compound of Si and Ti, such as a silicon-titanium alkoxide, may also be used.
  • the target may not be limited to a rod shape, and a plate-shaped substrate may be employed.
  • the porous TiO 2 —SiO 2 glass body is heated to a vitrification temperature for vitrification to obtain a vitrified TiO 2 —SiO 2 glass body.
  • the vitrification means a state where the porous glass body is densified to such an extent that void spaces can no longer be detected by an optical microscope
  • the vitrification temperature means the temperature at which the porous glass body can be densified until void can no longer be detected by an optical microscope.
  • the vitrification temperature is usually from 1,400 to 1,700° C., particularly preferably from 1,450 to 1,650° C.
  • the atmosphere is preferably an atmosphere of 100% inert gas such as helium or an atmosphere containing an inert gas such as helium, as the main component.
  • the pressure may be a reduced pressure or a normal pressure. Especially in the case of a normal pressure, helium gas may be employed. In the case of a reduced pressure, a pressure of at most 13,000 Pa is preferred. In this specification, “Pa” is meant for an absolute pressure i.e. not a gauge pressure.
  • the vitrified TiO 2 —SiO 2 glass body obtained in step (b) is heated to a temperature above near the softening temperature and formed into a desired shape to obtain a formed TiO 2 —SiO 2 glass body.
  • the temperature for forming is preferably from 1,500 to 1,800° C. If it is lower than 1,500° C., no substantial deadweight transformation takes place, since the viscosity of the TiO 2 —SiO 2 glass is high, and growth of cristobalite being a crystalline phase of SiO 2 or growth of rutile or anatase being a crystalline phase of TiO 2 takes place, thus leading to so-called devitrification. If the temperature exceeds 1,800° C., vaporization of SiO 2 tends to be not negligible.
  • the fictive temperature of the TiO 2 —SiO 2 glass is controlled by carrying out annealing treatment wherein the formed TiO 2 —SiO 2 glass body obtained in step (c) is held at a temperature of from 600 to 1,200° C. for at least 5 hours, and then, the temperature is lowered to not higher than 500° C. at an average cooling rate of at most 10° C./hr. After the temperature is lowered to not higher than 500° C., the glass body may be cooled.
  • the atmosphere in such a case is preferably an atmosphere of 100% inert gas such as helium, argon or nitrogen or an atmosphere containing such an inert gas as the main component, or an atmosphere of air, and the pressure is preferably a reduced pressure or a normal pressure.
  • TiO 2 —SiO 2 glass particles obtained by gasifying TiCl 4 and SiCl 4 as glass-forming materials for TiO 2 —SiO 2 glass, respectively, then mixing them and feeding them to heat hydrolysis (flame hydrolysis) in oxyhydrogen flame, were deposited and grown on a target made of quartz glass rotating at a rate of 25 rpm, to form a porous TiO 2 —SiO 2 glass body having a diameter of 80 mm and a length of about 100 mm (step (a)).
  • the obtained porous TiO 2 —SiO 2 glass body was heated to 1,550° C. in an atmosphere of 100% He and held at this temperature for 10 hours for vitrification to obtain a vitrified TiO 2 —SiO 2 glass body (step (b)).
  • the obtained vitrified TiO 2 —SiO 2 glass body was heated to 1,600° C. i.e. higher than the softening point for deadweight transformation and formed into a block shape of 50 mm ⁇ 50 mm ⁇ 10 mm (step (c)).
  • the obtained block was set in an electric furnace and held at 950° C. for 100 hours. Then, the temperature was lowered to 500° C. at a rate of 5° C./hr, and then the block was cooled to room temperature (step (d)) to obtain TiO 2 —SiO 2 glass.
  • Example 1 In the step (a) in Example 1, the TiO 2 —SiO 2 glass particles were deposited and grown on a target made of quartz glass rotating at a rate of 100 rpm. Other than this, in the same manner as in Example 1, TiO 2 —SiO 2 glass was obtained.
  • Example 1 In the step (a) in Example 1, the TiO 2 —SiO 2 glass particles were deposited and grown on a target made of quartz glass rotating at a rate of 250 rpm. Other than this, in the same manner as in Example 1, TiO 2 —SiO 2 glass was obtained.
  • Example 1 In the step (a) in Example 1, the TiO 2 —SiO 2 glass particles were deposited and grown on a target made of quartz glass rotating at a rate of 5 rpm. Other than this, in the same manner as in Example 1, TiO 2 —SiO 2 glass was obtained.
  • TiO 2 —SiO 2 glass particles obtained by gasifying TiCl 4 and SiCl 4 as glass-forming materials for TiO 2 —SiO 2 glass, respectively, then mixing them and feeding them to heat hydrolysis (flame hydrolysis) in oxyhydrogen flame, were deposited and grown on a target made of quartz glass rotating at a rate of 25 rpm, to form a porous TiO 2 —SiO 2 glass body having a diameter of 30 mm and a length of 80 cm (step (a)).
  • the obtained porous TiO 2 —SiO 2 glass body was heated to 1,430° C. in an atmosphere of 100% He and held at this temperature for 2 hours for vitrification to obtain a vitrified TiO 2 —SiO 2 glass body (step (b)).
  • step (c) it was heated to 1,680° C. i.e. higher than the softening point for deadweight transformation and formed into a block shape of 160 mm ⁇ 160 mm ⁇ 150 mm (step (c)). Then, it was sliced into a block of 7 mm in thickness. The obtained block of 160 mm ⁇ 160 mm ⁇ 7 mm was set in an electric furnace and held at 950° C. for 100 hours. Then, the temperature was lowered to 500° C. at a rate of 5° C./hr, and then the block was cooled to room temperature (step (d)) to obtain TiO 2 —SiO 2 glass.
  • Example 1 The evaluation was carried out in accordance with the above-mentioned measuring methods, respectively.
  • the results of evaluation of Examples 1 to 5 are summarized in Table 1.
  • Examples 1, 2, 3 and 5 are Examples of the present invention, and Example 4 is a Comparative Example.
  • the striae pitch is not more than 10 ⁇ m, and in at least one plane, the fluctuation of the refractive index in small areas is not more than 200 ppm, and the fluctuation of the TiO 2 concentration is not more than 0.06 mass %.
  • the fluctuation of the refractive index or the fluctuation of the TiO 2 concentration are attributable to the striae, and the strength of the striae is reduced in Examples 1 and 2, whereby MSFR can easily be reduced by polishing and it will be possible to be ultra smooth surface.
  • the fluctuation of the refractive index is not more than 200 ppm, and the fluctuation of the TiO 2 concentration is not more than 0.06 mass %.
  • Example 3 the presence of striae can be visually confirmed, and by the measurement microscope, the striae pitch was confirmed to be 1 ⁇ m, but the fluctuation of the refractive index could not be detected by the above-mentioned method. Accordingly, it is considered that the fluctuation of the refractive index is not more than 50 ppm, and the fluctuation of the TiO 2 concentration is not more than 0.06 mass %. Accordingly, in Example 3, MSFR can be reduced more easily, and it is possible to obtain ultra smooth surface.
  • the striae pitch is at least 10 ⁇ m
  • the fluctuation of the refractive index in small areas is at least 200 ppm
  • the fluctuation of the TiO 2 concentration is at least 0.06 mass %.
  • the degree of striae was very high, and it was difficult to reduce MSFR by polishing.
  • the fluctuation of the refractive index in a broad area is not more than 200 ppm, and it becomes possible to obtain an optical material for EUV lithography wherein the fluctuation of the refractive index ( ⁇ n) is at most 2 ⁇ 10 ⁇ 4 in a plane perpendicular to the incident light direction.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Manufacturing & Machinery (AREA)
  • Glass Compositions (AREA)
  • Glass Melting And Manufacturing (AREA)
US11/174,533 2003-04-03 2005-07-06 Silica glass containing TiO2 and optical material for EUV lithography Expired - Lifetime US7462574B2 (en)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
JP2003-100798 2003-04-03
JP2003100798 2003-04-03
JP2003-100799 2003-04-03
JP2003100799 2003-04-03
JP2004076312A JP5367204B2 (ja) 2003-04-03 2004-03-17 TiO2を含有するシリカガラスおよびEUVリソグラフィ用光学部材
JP2004-076312 2004-03-17
PCT/JP2004/004829 WO2004089838A1 (fr) 2003-04-03 2004-04-02 Verre de silice renfermant tio 2 et materiau optique pour lithographie dans l'ultraviolet extreme

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2004/004829 Continuation WO2004089838A1 (fr) 2003-04-03 2004-04-02 Verre de silice renfermant tio 2 et materiau optique pour lithographie dans l'ultraviolet extreme

Publications (2)

Publication Number Publication Date
US20050245383A1 US20050245383A1 (en) 2005-11-03
US7462574B2 true US7462574B2 (en) 2008-12-09

Family

ID=33162776

Family Applications (1)

Application Number Title Priority Date Filing Date
US11/174,533 Expired - Lifetime US7462574B2 (en) 2003-04-03 2005-07-06 Silica glass containing TiO2 and optical material for EUV lithography

Country Status (5)

Country Link
US (1) US7462574B2 (fr)
EP (1) EP1608599B2 (fr)
JP (1) JP5367204B2 (fr)
DE (1) DE602004009553T3 (fr)
WO (1) WO2004089838A1 (fr)

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070263281A1 (en) * 2005-12-21 2007-11-15 Maxon John E Reduced striae low expansion glass and elements, and a method for making same
US20090017257A1 (en) * 2006-04-12 2009-01-15 Asahi Glass Company, Limited Processing method of glass substrate, and highly flat and highly smooth glass substrate
US20090062102A1 (en) * 2007-08-31 2009-03-05 Nicholas Francis Borrelli Photomachinable glass compositions having tunable photosensitivity
US20100179047A1 (en) * 2009-01-13 2010-07-15 Asahi Glass Co., Ltd. Optical member comprising tio2-containing silica glass
US20100261597A1 (en) * 2007-12-27 2010-10-14 Asahi Glass Company Limited Tio2-containing silica glass
US20100323873A1 (en) * 2008-02-09 2010-12-23 Asahi Glass Company, Limited Tio2-containing silica glass and optical member for lithography using the same
US20110159413A1 (en) * 2009-12-25 2011-06-30 Shin-Etsu Chemical Co., Ltd. Titania-doped quartz glass and making method
US8012653B2 (en) 2008-08-01 2011-09-06 Asahi Glass Company, Limited Substrate for EUV mask blanks
US8034731B2 (en) 2008-02-25 2011-10-11 Asahi Glass Company, Limited TIO2-containing silica glass and optical member for lithography using the same
US8039409B2 (en) 2008-04-16 2011-10-18 Asahi Glass Company, Limited TiO2-containing silica glass for optical member for EUV lithography
US8093165B2 (en) 2008-02-27 2012-01-10 Asahi Glass Company, Limited TiO2-containing silica glass and optical member for EUV lithography using the same
US8178450B2 (en) 2008-02-26 2012-05-15 Asahi Glass Company, Limited TiO2-containing silica glass and optical member for EUV lithography using high energy densities as well as special temperature controlled process for its manufacture
WO2014036116A1 (fr) 2012-08-30 2014-03-06 Corning Incorporated Verre de silice-oxyde de titane dopé par du niobium et procédé de préparation
EP2757078A1 (fr) 2013-01-22 2014-07-23 Shin-Etsu Chemical Co., Ltd. Élément de lithographie EUV, son procédé de fabrication et verre de quartz dopé au titane
US8820122B2 (en) 2010-09-02 2014-09-02 Shin-Etsu Chemical Co., Ltd. Titania-doped quartz glass and making method
US9296636B2 (en) 2011-04-11 2016-03-29 Shin-Etsu Chemical Co., Ltd. Titania doped quartz glass and making method
US11378737B2 (en) * 2017-10-06 2022-07-05 Sumitomo Electric Industries, Ltd. Optical fiber preform, method for manufacturing optical fiber preform, and method for setting striae pitch of optical fiber preform

Families Citing this family (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7428037B2 (en) * 2002-07-24 2008-09-23 Carl Zeiss Smt Ag Optical component that includes a material having a thermal longitudinal expansion with a zero crossing
JP5367204B2 (ja) 2003-04-03 2013-12-11 旭硝子株式会社 TiO2を含有するシリカガラスおよびEUVリソグラフィ用光学部材
JP4792706B2 (ja) * 2003-04-03 2011-10-12 旭硝子株式会社 TiO2を含有するシリカガラスおよびその製造方法
JP4492123B2 (ja) * 2004-01-05 2010-06-30 旭硝子株式会社 シリカガラス
US8841377B2 (en) 2004-05-13 2014-09-23 Asahi Fiber Glass Company, Limited Glass fiber for reinforcing polycarbonate resin and polycarbonate resin formed article
WO2006004169A1 (fr) * 2004-07-01 2006-01-12 Asahi Glass Company, Limited Verre de silice au tio2 et son procede de fabrication
US7713632B2 (en) 2004-07-12 2010-05-11 Cardinal Cg Company Low-maintenance coatings
JP4568225B2 (ja) * 2004-12-24 2010-10-27 信越石英株式会社 脈理のないシリカ・チタニアガラスの製造方法
JP4487783B2 (ja) * 2005-01-25 2010-06-23 旭硝子株式会社 TiO2を含有するシリカガラスの製造方法およびTiO2を含有するシリカガラスを用いたEUVリソグラフィ用光学部材
JP4646314B2 (ja) * 2005-02-01 2011-03-09 信越石英株式会社 均質なシリカ・チタニアガラスの製造方法
JP4568219B2 (ja) * 2005-02-01 2010-10-27 信越石英株式会社 均質なシリカ・チタニアガラスの製造方法
EP1924533A1 (fr) * 2005-09-16 2008-05-28 Asahi Glass Company, Limited Verre de silice et matériau optique
JP5035516B2 (ja) 2005-12-08 2012-09-26 信越化学工業株式会社 フォトマスク用チタニアドープ石英ガラスの製造方法
US20070137252A1 (en) * 2005-12-21 2007-06-21 Maxon John E Reduced striae low expansion glass and elements, and a method for making same
US7862910B2 (en) 2006-04-11 2011-01-04 Cardinal Cg Company Photocatalytic coatings having improved low-maintenance properties
US7313957B1 (en) * 2006-06-15 2008-01-01 The Yokohama Rubber Co., Ltd. Apparatus, method and program for evaluating work characteristic
US20080011599A1 (en) 2006-07-12 2008-01-17 Brabender Dennis M Sputtering apparatus including novel target mounting and/or control
JP5169163B2 (ja) * 2006-12-01 2013-03-27 旭硝子株式会社 予備研磨されたガラス基板表面を仕上げ加工する方法
JP5042714B2 (ja) * 2007-06-06 2012-10-03 信越化学工業株式会社 ナノインプリントモールド用チタニアドープ石英ガラス
JP2009013048A (ja) * 2007-06-06 2009-01-22 Shin Etsu Chem Co Ltd ナノインプリントモールド用チタニアドープ石英ガラス
KR101479804B1 (ko) * 2007-09-13 2015-01-06 아사히 가라스 가부시키가이샤 TiO2 함유 석영 유리 기판
US7820296B2 (en) 2007-09-14 2010-10-26 Cardinal Cg Company Low-maintenance coating technology
JP5369640B2 (ja) * 2008-02-19 2013-12-18 旭硝子株式会社 Euvl用光学部材、およびその平滑化方法
JP5202141B2 (ja) * 2008-07-07 2013-06-05 信越化学工業株式会社 チタニアドープ石英ガラス部材及びその製造方法
JP5287271B2 (ja) * 2009-01-13 2013-09-11 旭硝子株式会社 TiO2を含有するシリカガラスの成型方法およびそれによって成型されたEUVリソグラフィ用光学部材
KR101740067B1 (ko) * 2009-01-13 2017-05-25 아사히 가라스 가부시키가이샤 TiO₂를 함유하는 실리카 유리를 포함하는 광학 부재
CN102421713A (zh) 2009-05-13 2012-04-18 旭硝子株式会社 TiO2-SiO2玻璃体的制造方法及热处理方法、TiO2-SiO2玻璃体、EUVL用光学基材
JP2012181220A (ja) * 2009-07-02 2012-09-20 Asahi Glass Co Ltd ArFリソグラフィ用ミラー、およびArFリソグラフィ用光学部材
JPWO2011021609A1 (ja) * 2009-08-19 2013-01-24 旭硝子株式会社 TiO2を含有するシリカガラスおよびEUVリソグラフィ用光学部材
US8713969B2 (en) * 2009-08-31 2014-05-06 Corning Incorporated Tuning Tzc by the annealing of ultra low expansion glass
EP2518030A4 (fr) * 2009-12-01 2013-09-11 Asahi Glass Co Ltd Verre de silice contenant du tio2
JP2011132065A (ja) * 2009-12-24 2011-07-07 Asahi Glass Co Ltd 多孔質石英ガラス体の製造方法
CN103003054B (zh) * 2010-07-12 2014-11-19 旭硝子株式会社 压印模具用含TiO2石英玻璃基材及其制造方法
US20120026473A1 (en) 2010-07-29 2012-02-02 Michael Lucien Genier Highly reflective, hardened silica titania article and method of making
JP2011051893A (ja) * 2010-11-29 2011-03-17 Shin-Etsu Chemical Co Ltd ナノインプリントモールド用チタニアドープ石英ガラス
EP2671848A1 (fr) 2011-01-31 2013-12-11 Asahi Glass Company, Limited Méthode de production de corps en verre de silice contenant du titane, et corps en verre de silice contenant du titane
WO2013084978A1 (fr) * 2011-12-09 2013-06-13 信越石英株式会社 Substrat de masque photographique pour lithographie par ultraviolets extrêmes de verre de dioxyde de titane-silice
US9382151B2 (en) * 2014-01-31 2016-07-05 Corning Incorporated Low expansion silica-titania articles with a Tzc gradient by compositional variation
JP6572688B2 (ja) * 2015-09-02 2019-09-11 Agc株式会社 インプリントモールド用ガラス板、およびインプリントモールド用ガラス板の製造方法
WO2018093985A1 (fr) 2016-11-17 2018-05-24 Cardinal Cg Company Technologie de revêtement à dissipation statique
DE102016224236A1 (de) 2016-12-06 2017-01-26 Carl Zeiss Smt Gmbh Rohling aus TiO2-dotiertem Quarzglas, optisches Element für die EUV-Lithographie und EUV-Lithographiesystem damit

Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0293064A2 (fr) 1987-05-29 1988-11-30 Corning Glass Works Méthode sol-gel pour fabriquer un verre à expansion extrêmement faible
US5696038A (en) 1995-09-12 1997-12-09 Corning Incorporated Boule oscillation patterns in methods of producing fused silica glass
WO1998000372A2 (fr) 1996-06-17 1998-01-08 Corning Incorporated Procede de formation de preformes contenant de l'oxyde de titane et d'ebauches de verre de silice
EP0901989A1 (fr) 1997-09-11 1999-03-17 Nikon Corporation Verre de silice et procédé de sa fabrication
US5970751A (en) 1998-09-22 1999-10-26 Corning Incorporated Fused SiO2 -TiO2 glass method
WO2002032622A1 (fr) 2000-10-13 2002-04-25 Corning Incorporated Procede permettant d'eviter les stries dans des miroirs de lithographie a uv extreme
US6465272B1 (en) 1999-07-22 2002-10-15 Corning Incorporated Extreme ultraviolet soft x-ray projection lithographic method and mask devices
US20020157421A1 (en) * 2001-04-27 2002-10-31 Ackerman Bradford G. Method for producing titania-doped fused silica glass
US6499315B1 (en) 1997-04-08 2002-12-31 Shin-Etsu Quartz Products Co., Ltd Production method for making an optical member for excimer laser using synthetic quartz glass
US20030159464A1 (en) 2002-02-27 2003-08-28 Bowden Bradley F. High purity glass bodies formed by zero shrinkage casting
WO2003077038A2 (fr) 2002-03-05 2003-09-18 Corning Incorporated Elements a rayonnement ultraviolet extreme a stries reduites
WO2003076352A2 (fr) 2002-03-05 2003-09-18 Corning Incorporated Procede de fabrication d'elements ultraviolets extremes de silice-dioxyde de titane
US20050245383A1 (en) 2003-04-03 2005-11-03 Asahi Glass Company Limited Silica glass containing TiO2 and optical material for EUV lithography

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63162538A (ja) * 1986-12-24 1988-07-06 Fujikura Ltd 石英系ロツドレンズの製造方法
JP3944759B2 (ja) * 1997-04-08 2007-07-18 信越石英株式会社 光学用合成石英ガラス、その製造方法およびエキシマレーザー用光学部材
JP3893816B2 (ja) * 1998-10-28 2007-03-14 旭硝子株式会社 合成石英ガラスおよびその製造方法

Patent Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0293064A2 (fr) 1987-05-29 1988-11-30 Corning Glass Works Méthode sol-gel pour fabriquer un verre à expansion extrêmement faible
US5696038A (en) 1995-09-12 1997-12-09 Corning Incorporated Boule oscillation patterns in methods of producing fused silica glass
WO1998000372A2 (fr) 1996-06-17 1998-01-08 Corning Incorporated Procede de formation de preformes contenant de l'oxyde de titane et d'ebauches de verre de silice
US6499315B1 (en) 1997-04-08 2002-12-31 Shin-Etsu Quartz Products Co., Ltd Production method for making an optical member for excimer laser using synthetic quartz glass
EP0901989A1 (fr) 1997-09-11 1999-03-17 Nikon Corporation Verre de silice et procédé de sa fabrication
US5970751A (en) 1998-09-22 1999-10-26 Corning Incorporated Fused SiO2 -TiO2 glass method
US6465272B1 (en) 1999-07-22 2002-10-15 Corning Incorporated Extreme ultraviolet soft x-ray projection lithographic method and mask devices
US6576380B2 (en) 1999-07-22 2003-06-10 Corning Incorporated Extreme ultraviolet soft x-ray projection lithographic method and mask devices
WO2002032622A1 (fr) 2000-10-13 2002-04-25 Corning Incorporated Procede permettant d'eviter les stries dans des miroirs de lithographie a uv extreme
WO2002088036A1 (fr) 2001-04-27 2002-11-07 Corning Incorporated Procede de production de substrats de verre a base de dioxyde de titane et de silice fondue destines a la lithographie par ultraviolets extremes
US20020157421A1 (en) * 2001-04-27 2002-10-31 Ackerman Bradford G. Method for producing titania-doped fused silica glass
US20030159464A1 (en) 2002-02-27 2003-08-28 Bowden Bradley F. High purity glass bodies formed by zero shrinkage casting
WO2003077038A2 (fr) 2002-03-05 2003-09-18 Corning Incorporated Elements a rayonnement ultraviolet extreme a stries reduites
WO2003076352A2 (fr) 2002-03-05 2003-09-18 Corning Incorporated Procede de fabrication d'elements ultraviolets extremes de silice-dioxyde de titane
US20030226377A1 (en) * 2002-03-05 2003-12-11 Barrett W. Tim Method of making silica-titania extreme ultraviolet elements
US7053017B2 (en) * 2002-03-05 2006-05-30 Corning Incorporated Reduced striae extreme ultraviolet elements
US20050245383A1 (en) 2003-04-03 2005-11-03 Asahi Glass Company Limited Silica glass containing TiO2 and optical material for EUV lithography

Non-Patent Citations (25)

* Cited by examiner, † Cited by third party
Title
B. Ackerman et al., "Improved Characteristics of ULE(R) Glass for Meeting EUV Lithograph Needs", Poster Session, 1st International EUV Lithography Symposium, Dallas, Texas, Oct. 15-17, 2002.
Bradford Ackerman, et al., "An Old Material Finds a New Application," Laser Focus World v38 (11) 2002, pp. 109-113. Note: p. 9 indicates the document was received Nov. 1, 2002.
Christine Heckle, et al., "Development of Mask Materials for EUVL", Proc. SPIE v4889 (2002) pp. 1113-1120, no month.
Corning Code 7971, Titanium Silicate Zero Expansion Material, Glass Bulletin, 2000, no month.
Corning Code 7971, ULE Titanium Silicate, Glass Bulletin 1985, Corning Glass Works, Corning, N.Y. 14831, 1985, no month.
D15A. Quotation to Customer 1 dated Feb. 26, 2003 for sale of Corning 7972 ULE EUV Grade glass having a CTE of 0± 5ppb/ °C.
D15B. Closed order for Customer 1 dated Mar. 2003 for a shipped order of Corning [7972] ULE EUV Grade glass having a CTE of 0 ± 5 ppb/ °C.
D16A. Quotation to Customer 2 dated Apr. 1, 2003 for sale of Corning 7972 ULE EUV Grade glass.
D16B. Closed order for Customer 2 dated Apr. 7, 2003 for a shipped order of Corning [7972] ULE EUV Grade glass.
D17. Affidavit of Junichi Yokoyama regarding offers to sell Corning ULE(R) EUV glass (D15 and D16), Jul. 11, 2008.
D18. Affidavit of Kenneth E. Hrdina regarding the availability to the public of D4A and D5 and regarding Corning ULE(R) EUV Grade glass, Jul. 16, 2008.
D19. Affidavit of Walter M. Douglas regarding identification of the ULE(R) EUV glass (D15 and D16), Jul. 16, 2008.
G. J. Copley, et al., "The influence of Titania upon the Thermal Expansion of Vitreous Silica", Physics and Chemistry of Glasses, vol. 14, No. 4, Aug. (1973), pp. 73-76.
Henry E. Hagy, "High Precision Photoelastic and Ultrasonic Techniques for Determining Absolute and Differential Thermal Expansion of Titania-Silica Glasses," Applied Optics, vol. 12, No. 7, Jul. 1973, pp. 1440-1446.
Henry E. Hagy, et al., "Determining absolute thermal expansion of titania-silica glasses: a refined ultrasonic method," Applied Optics, vol. 14 No. 9, Sep. 1975, pp. 2099-2103.
Hrdina et al., "Measuring and Tailoring CTE within ULE(R) Glass," Proc. SPIE v5037 (2003), pp. 227-235. Presented at Emerging Lithographic Technologies VII Conference, Santa Clara, CA Feb. 25, 2003.
Kenneth E. Hrdian, et al., "Characterization and Characteristics of a ULE(R) Glass Tailored for EUVL Needs", Proc. SPIE v4688 (2002), pp. 454-461, Presented at Emerging Lithographic Technologies VI, Santa Clara, CA, Mar. 3-8, 2002.
Phil Fenn, et al., "Characterization and Characteristics of a ULE(R) Glass Tailored for EUVL Needs", Poster Session: ML4688-52, Presented at Emerging Lithographic Technologies VI, Santa Clara, CA, Mar. 3-8, 2002.
U.S. Appl. No. 11/172,872, filed Jul. 5, 2005, Iwahashi, et al.
U.S. Appl. No. 11/172,950, filed Jul. 5, 2002, Iwahashi, et al.
U.S. Appl. No. 11/174,533, filed Jul. 6, 2005, Iwahashi, et al.
U.S. Appl. No. 11/435,887, filed May 18, 2006, Iwahashi, et al.
U.S. Appl. No. 11/589,875, filed Oct. 31, 2006, Koike, et al.
U.S. Appl. No. 11/957,855, filed Dec. 17, 2007, Iwahashi, et al.
William M. Tong, et al., "Mask substrate requirements and development for extreme ultraviolet lithography (EUVL)", Proc. SPIE vol. 3873 (1999). pp. 412-428, no month.

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070263281A1 (en) * 2005-12-21 2007-11-15 Maxon John E Reduced striae low expansion glass and elements, and a method for making same
US20090017257A1 (en) * 2006-04-12 2009-01-15 Asahi Glass Company, Limited Processing method of glass substrate, and highly flat and highly smooth glass substrate
US8137574B2 (en) * 2006-04-12 2012-03-20 Asahi Glass Company, Limited Processing method of glass substrate, and highly flat and highly smooth glass substrate
US20090062102A1 (en) * 2007-08-31 2009-03-05 Nicholas Francis Borrelli Photomachinable glass compositions having tunable photosensitivity
US7799711B2 (en) * 2007-08-31 2010-09-21 Corning Incorporated Photomachinable glass compositions having tunable photosensitivity
US20100261597A1 (en) * 2007-12-27 2010-10-14 Asahi Glass Company Limited Tio2-containing silica glass
US7989378B2 (en) 2007-12-27 2011-08-02 Asahi Glass Company, Limited TiO2-containing silica glass
US20100323873A1 (en) * 2008-02-09 2010-12-23 Asahi Glass Company, Limited Tio2-containing silica glass and optical member for lithography using the same
US8034731B2 (en) 2008-02-25 2011-10-11 Asahi Glass Company, Limited TIO2-containing silica glass and optical member for lithography using the same
US8178450B2 (en) 2008-02-26 2012-05-15 Asahi Glass Company, Limited TiO2-containing silica glass and optical member for EUV lithography using high energy densities as well as special temperature controlled process for its manufacture
US8093165B2 (en) 2008-02-27 2012-01-10 Asahi Glass Company, Limited TiO2-containing silica glass and optical member for EUV lithography using the same
US7998892B2 (en) 2008-02-29 2011-08-16 Asahi Glass Company, Limited TiO2-containing silica glass and optical member for lithography using the same
US8039409B2 (en) 2008-04-16 2011-10-18 Asahi Glass Company, Limited TiO2-containing silica glass for optical member for EUV lithography
US8012653B2 (en) 2008-08-01 2011-09-06 Asahi Glass Company, Limited Substrate for EUV mask blanks
US20100179047A1 (en) * 2009-01-13 2010-07-15 Asahi Glass Co., Ltd. Optical member comprising tio2-containing silica glass
US8735308B2 (en) 2009-01-13 2014-05-27 Asahi Glass Company, Limited Optical member comprising TiO2-containing silica glass
US20110159413A1 (en) * 2009-12-25 2011-06-30 Shin-Etsu Chemical Co., Ltd. Titania-doped quartz glass and making method
US9746773B2 (en) 2009-12-25 2017-08-29 Shin-Etsu Chemical Co., Ltd. Titania-doped quartz glass and making method
US8820122B2 (en) 2010-09-02 2014-09-02 Shin-Etsu Chemical Co., Ltd. Titania-doped quartz glass and making method
US9296636B2 (en) 2011-04-11 2016-03-29 Shin-Etsu Chemical Co., Ltd. Titania doped quartz glass and making method
US10114280B2 (en) 2011-04-11 2018-10-30 Shin-Etsu Chemical Co., Ltd. Titania-doped quartz glass and making method
WO2014036116A1 (fr) 2012-08-30 2014-03-06 Corning Incorporated Verre de silice-oxyde de titane dopé par du niobium et procédé de préparation
EP2757078A1 (fr) 2013-01-22 2014-07-23 Shin-Etsu Chemical Co., Ltd. Élément de lithographie EUV, son procédé de fabrication et verre de quartz dopé au titane
US9278881B2 (en) 2013-01-22 2016-03-08 Shin-Etsu Chemical Co., Ltd. EUV lithography member, making method, and titania-doped quartz glass
US11378737B2 (en) * 2017-10-06 2022-07-05 Sumitomo Electric Industries, Ltd. Optical fiber preform, method for manufacturing optical fiber preform, and method for setting striae pitch of optical fiber preform

Also Published As

Publication number Publication date
DE602004009553D1 (de) 2007-11-29
DE602004009553T3 (de) 2014-10-09
JP5367204B2 (ja) 2013-12-11
EP1608599B1 (fr) 2007-10-17
WO2004089838A1 (fr) 2004-10-21
DE602004009553T2 (de) 2008-07-31
US20050245383A1 (en) 2005-11-03
EP1608599A1 (fr) 2005-12-28
JP2004315351A (ja) 2004-11-11
EP1608599B2 (fr) 2014-08-06

Similar Documents

Publication Publication Date Title
US7462574B2 (en) Silica glass containing TiO2 and optical material for EUV lithography
EP1608598B2 (fr) Verre de silice renfermant tio sb 2 /sb et son procede de production
US7538052B2 (en) Silica glass containing TiO2 and process for its production
US20070207911A1 (en) Process for producing silica glass containing tio2, and optical material for euv lithography employing silica glass containing tio2
US7989378B2 (en) TiO2-containing silica glass
US7998892B2 (en) TiO2-containing silica glass and optical member for lithography using the same
US20100323871A1 (en) Tio2-containing silica glass and optical member for euv lithography using high energy densities as well as special temperature controlled process for its manufacture
JP5716730B2 (ja) TiO2を含有するシリカガラスおよびEUVリソグラフィ用光学部材
JP5733350B2 (ja) TiO2を含有するシリカガラスおよびその製造法
JP5402975B2 (ja) TiO2を含有するシリカガラスおよびその製造法

Legal Events

Date Code Title Description
AS Assignment

Owner name: ASAHI GLASS COMPANY, LIMITED, JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:IWAHASHI, YASUTOMI;KOIKE, AKIO;REEL/FRAME:016756/0209;SIGNING DATES FROM 20050614 TO 20050617

STCF Information on status: patent grant

Free format text: PATENTED CASE

FPAY Fee payment

Year of fee payment: 4

FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

FPAY Fee payment

Year of fee payment: 8

AS Assignment

Owner name: AGC INC., JAPAN

Free format text: CHANGE OF NAME;ASSIGNOR:ASAHI GLASS COMPANY, LIMITED;REEL/FRAME:046730/0786

Effective date: 20180701

MAFP Maintenance fee payment

Free format text: PAYMENT OF MAINTENANCE FEE, 12TH YEAR, LARGE ENTITY (ORIGINAL EVENT CODE: M1553); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

Year of fee payment: 12